Agonist-Antagonist Actions and Stereoselectivity of Optical Pairs of Some N-substituted α-N-Normetazocines
作者:Mario D. Aceto、Everette L. May、Louis S. Harris、Arthur E. Jacobson、Hiroyoshi Awaya
DOI:10.1002/jps.2600731260
日期:1984.12
(-)-N-allyl-N-normetazocine (SKF 10,047; NANM). The propynyl isomers (IIIa and b) display profiles of activity more closely like the corresponding isomers of metazocine. Evidence is considered which suggests that some of the (+)-isomers merit closer scrutiny in animal and human studies.
α-(-)-,(+)-和(+/-)-N-4-甲基戊基-,(-)-和(+)-N-顺式-3-氯烯丙基-和(-)-和(+)-N-丙炔基-N-去甲恶嗪碱(分别为I,II和III)是由α-(-)-,(+)-和(+/-)-N-去甲恶嗪碱(IV)制备的并测试了小鼠和吗啡依赖性恒河猴的抗伤害感受活性。用Ia和b得到的结果与用相应的吩唑嗪异构体得到的结果有点相似,而用IIa和b观察到的结果更接近于(+)-和(-)-N-烯丙基-N-去甲三嗪(SKF)的报道。 10047; NANM)。丙炔基异构体(IIIa和b)显示的活性分布更紧密,类似于间苯二酚的相应异构体。认为有证据表明,一些(+)异构体在动物和人体研究中值得进一步研究。